Canonical Allele Identifier: PA645471549
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 428538
ClinVar RCV Id: RCV000491136 RCV000810636 RCV004003473
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Phe131Val
CA038462
NM_000251.3:c.391T>G